Canonical Allele Identifier: PA2499235841
Gene: SUOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1055636
ClinVar RCV Id: RCV002254641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027559.1:p.Val166Ile
CA385284090
NM_001032387.2:c.496G>A